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Connection

FERNANDO SCAGLIA to Phenylketonurias

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This is a "connection" page, showing publications FERNANDO SCAGLIA has written about Phenylketonurias.
FERNANDO SCAGLIA
Connection Strength
0.273
Phenylketonurias
  1. Developmental and Phenotypic Outcomes in Mild Phenylalanine Hydroxylase Deficiency. Am J Med Genet A. 2026 Aug; 200(8):1814-1820.
    View in: PubMed
    Score: 0.235
  2. Psychiatric symptoms of inherited metabolic disease. J Inherit Metab Dis. 2000 Feb; 23(1):2-6.
    View in: PubMed
    Score: 0.038
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.